Classifications

• • C—CHEMISTRY; METALLURGY
  • C01—INORGANIC CHEMISTRY
  • C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
  • C01B7/00—Halogens; Halogen acids
  • C01B7/01—Chlorine; Hydrogen chloride
  • C01B7/03—Preparation from chlorides
  • C01B7/04—Preparation of chlorine from hydrogen chloride
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
  • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
  • B01J23/00—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
  • B01J23/38—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of noble metals
  • B01J23/40—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of noble metals of the platinum group metals
  • B01J23/46—Ruthenium, rhodium, osmium or iridium
  • B01J23/462—Ruthenium
• • C—CHEMISTRY; METALLURGY
  • C01—INORGANIC CHEMISTRY
  • C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
  • C01B7/00—Halogens; Halogen acids

Definitions

• the invention relates to a fixed bed process for the production of chlorine by catalytic gas phase oxidation of hydrogen chloride.
• EP-B 0 233 773 describes the catalytic oxidation of hydrogen chloride over powdered chromium oxide catalysts in a fluidized bed process.
• Fluidized bed processes are characterized by the possibility of very isothermal temperature control.
• the formation of local overheating of the catalyst bed the formation of so-called "hot spots", can be largely avoided.
• fluidized bed processes have disadvantages. These include the difficulties with up-scaling, a sometimes considerable discharge of catalyst material with the reaction gases during the operation of the Fluidized bed reactors, and the instability of the fluidized bed caused by sticking of catalyst particles.
• Fixed bed processes do not have the disadvantages mentioned.
• tray reactors with intermediate cooling or tube-bundle reactors are used.
• EP-A 0 936 184 describes the implementation of the Deacon reaction on a fixed catalyst bed using ruthenium catalysts. When exothermic reactions are carried out on a fixed catalyst bed, however, hot spots are generally formed.
• the object of the invention is to provide an improved process for the production of chlorine from hydrogen chloride which overcomes the disadvantages of the prior art.
• the object is achieved by a process for the production of chlorine by catalytic gas-phase oxidation of hydrogen chloride on a fixed catalyst bed with the steps:
• a feed gas stream I containing hydrogen chloride and an oxygen feed gas stream II are provided;
• a feed gas stream of earth-borne hydrogen chloride is provided.
• Hydrogen chloride is obtained, for example, in the production of aromatic polyisocyanates such as tolylene diisocyanate and diphenylmethane diisocyanate (MDI) from the corresponding polyamines and phosgene, in the production of acid chlorides, in the chlorination of aromatics, in the production of vinyl chloride and in the production of polycarbonates.
• This hydrogen chloride can contain hydrocarbons or chlorinated hydrocarbons as impurities, for example in amounts of 100 to 3000 ppm.
• other gas constituents can be contained, such as carbon monoxide, carbon dioxide, nitrogen and other inert gases, typically in amounts of 0 to 1% by volume.
• the contaminants can be removed, for example, by catalytic combustion of the hydrocarbons and chlorohydrocarbons in the feed gas stream or by absorption of the hydrocarbons and chlorohydrocarbons in a suitable absorbent from the feed gas stream.
• the feed gas stream II can consist of pure oxygen, technical oxygen, for example 94 vol.% Or 98 vol.% Technical oxygen, air or other oxygen / inert gas mixtures. Air is less preferred due to the high proportion of inert gas, pure oxygen for cost reasons.
• a process step b at least the feed gas stream I, the feed gas stream II and a backflow stream III are fed into an oxidation zone and hydrogen chloride is oxidized to chlorine in the presence of a catalyst arranged in a fixed bed, a product gas stream IV being obtained, the chlorine, unreacted oxygen, contains unreacted hydrogen chloride and water vapor.
• the backflow III is taken from the product gas stream IV formed in the catalytic oxidation of hydrogen chloride.
• the return stream III is taken from the product gas outlet IV and returned to the oxidation zone, a product gas stream IVa remaining.
• the backflow HI which already contains the products of the catalytic oxidation of hydrogen chloride, chlorine and water vapor, dilutes the feed gas mixture fed to the catalytic oxidation of hydrogen chloride by portions which are inert (chlorine and water vapor). As a result, the exothermic nature of the reaction is distributed over a larger gas volume flow. The dilution counteracts in particular the formation of hot spots. Because of the large heat capacity, the presence of water vapor in the feed gas mixture of catalytic hydrogen chloride oxidation is particularly advantageous.
• the ratio of the recycle stream III to the remaining product gas stream IVa is from 0.005 to 3, preferably from 0.2 to 1.5 and particularly preferably from 0.4 to 1.
• the return flow III can be returned by means of a compressor. If the pressure drop across the fixed catalyst bed is low, the use of a blower can also be sufficient. If the feed gas flow I, II and / or the return flow Ila are under an increased pressure, for example of> 5 bar, a propulsion jet nozzle can be used for the return, by means of which the return flow III is sucked in by one or more of the gas flows I, II or Ila.
• the recycle stream III can thus consist of several streams.
• the feed gas stream II contains technical oxygen, which is obtained by air liquefaction and is therefore under a high intrinsic pressure, and the return stream III is sucked in by the feed gas stream II by means of a propulsion jet nozzle.
• the technical oxygen obtained by air liquefaction can be under its own pressure of 30 bar or more.
• hydrogen chloride is oxidized to chlorine with oxygen in an exothermic equilibrium reaction, with water vapor being produced.
• Usual reaction temperatures are between 150 and 500 ° C, usual reaction pressures are between 1 and 25 bar. Since it is an equilibrium reaction, it is advisable to work at the lowest possible temperatures at which the catalyst still has sufficient activity.
• oxygen in excess of stoichiometric amounts. For example, a two to four-fold excess of oxygen is common. Since there is no fear of loss of selectivity, it can be economically advantageous to work at relatively high pressures and, accordingly, with longer residence times compared to normal pressure.
• Suitable catalysts contain ruthenium oxide, ruthenium chloride or other ruthenium compounds on silicon dioxide, aluminum oxide, titanium dioxide or zirconium dioxide as supports. Suitable catalysts can be obtained, for example, by applying ruthenium chloride to the support and then drying or drying and calcining. In addition to or instead of a ruthenium compound, suitable catalysts can also contain compounds of other noble metals, for example gold, palladium, platinum, osmium, iridium, silver, copper or rhenium. Suitable catalysts can also contain chromium (III) oxide.
• the catalytic hydrogen chloride oxidation is carried out in one or more fixed bed reactors.
• the hydrogen chloride oxidation can be carried out in several stages.
• the catalytic hydrogen chloride oxidation can be adiabatic or preferably isothermal or approximately isothermal, discontinuous, preferably continuously as a fixed bed process, preferably in tube bundle reactors over heterogeneous catalysts at reactor temperatures of 180 to 500 ° C, preferably 200 to 400 ° C, particularly preferably 220 to 350 ° C and a pressure of 1 to 25 bar, preferably 1.2 to 20 bar, particularly preferably 1.5 to 17 bar and in particular 2.0 to 15 bar.
• the isothermal or approximately isothermal procedure it is also possible to use a plurality of, that is to say 2 to 10, preferably 2 to 6, particularly preferably 2 to 5, in particular 2 to 3, reactors connected in series with additional intermediate cooling.
• the oxygen can either be added completely together with the hydrogen chloride before the first reactor or distributed over the various reactors. This series connection of individual reactors can also be combined in one apparatus.
• a preferred embodiment consists in using a structured catalyst bed in which the catalyst activity increases in the direction of flow.
• Such structuring of the catalyst bed can be carried out by impregnating the catalyst support with an active composition or by diluting the catalyst differently with an inert material.
• rings, cylinders or balls made of titanium dioxide, zirconium dioxide or mixtures thereof, aluminum oxide, steatite, ceramic, glass, graphite or stainless steel can be used as the inert material.
• the inert material should preferably have similar external dimensions.
• Arbitrary shapes are suitable as shaped catalyst bodies, tablets, rings, cylinders, stars, wagon wheels or balls are preferred, and rings, cylinders or star strands are particularly preferred.
• Suitable heterogeneous catalysts are, in particular, ruthenium compounds or copper compounds on support materials, which can also be doped; preference is given to optionally doped ruthenium catalysts.
• Suitable carrier materials are, for example, silicon dioxide, graphite, titanium dioxide with a rutile or anatase structure, zirconium dioxide, aluminum oxide or mixtures thereof, preferably titanium dioxide, zirconium dioxide, aluminum oxide or mixtures thereof, particularly preferably ⁇ - or ⁇ -aluminum oxide or mixtures thereof.
• the supported copper or ruthenium catalysts can be obtained, for example, by impregnating the support material with aqueous solutions of CuCl 2 or RuCl 3 and optionally a promoter for doping, preferably in the form of their chlorides, can be hardened.
• the catalyst can be shaped after or preferably before the support material is impregnated.
• Suitable promoters for doping are alkali metals such as lithium, sodium, potassium, rubidium and cesium, preferably lithium, sodium and potassium, particularly preferably potassium, alkaline earth metals such as magnesium, calcium, strontium and barium, preferably magnesium and calcium, particularly preferably magnesium, rare earth metals such as Scandium, yttrium, lanthanum, cerium, praseodymium and neodymium, preferably scandium, yttrium, lanthanum and cerium, particularly preferably lanthanum and cerium, or mixtures thereof.
• alkali metals such as lithium, sodium, potassium, rubidium and cesium, preferably lithium, sodium and potassium, particularly preferably potassium, alkaline earth metals such as magnesium, calcium, strontium and barium, preferably magnesium and calcium, particularly preferably magnesium, rare earth metals such as Scandium, yttrium, lanthanum, cerium, praseodymium and neodymium, preferably scandium,
• the moldings can then be dried at temperatures of 100 to 400 ° C., preferably 100 to 300 ° C., for example under a nitrogen, argon or air atmosphere and optionally calcined.
• the moldings are preferably first dried at 100 to 150 ° C. and then calcined at 200 to 400 ° C.
• the conversion of hydrogen chloride in a single pass can be limited to 15 to 95%, preferably 40 to 90%. After separation, unreacted hydrogen chloride can be partially or completely recycled into the catalytic hydrogen chloride oxidation.
• the volume ratio of hydrogen chloride to oxygen at the reactor inlet is generally between 1: 1 and 20: 1, preferably between 2: 1 and 8: 1, particularly preferably between 2: 1 and 5: 1.
• the process according to the invention preferably comprises further process steps of separating the product gas mixture and purifying the individual components. Usually, steps d) to g) are additionally carried out, d) hydrogen chloride and water being separated off from the product gas stream IVa, a gas stream V being obtained;
• the chlorine-containing product stream VI is further purified.
• unreacted hydrogen chloride and water vapor are separated off from the product gas stream IVa. This can be done by condensing aqueous hydrochloric acid from the product gas stream IVa by cooling. Hydrogen chloride can also be absorbed in dilute hydrochloric acid or water.
• separation step d) is carried out as described below.
• a process stage dl the product gas stream IVa is brought into contact with dilute hydrochloric acid of the concentration cl in an absorption zone and hydrogen chloride is absorbed in the dilute hydrochloric acid, a hydrochloric acid of the concentration c2 and a gas stream V which contains chlorine and oxygen being obtained.
• process step d2) the absorbed hydrogen chloride is released again from the hydrochloric acid of concentration c2 in a desorption zone.
• the released hydrogen chloride can be recycled, at least partially, preferably completely, as the backflow Ia containing hydrogen chloride into the oxidation zone, where further chlorine is obtained from the recycled hydrogen chloride.
• a dilute hydrochloric acid of concentration cl is recovered as an absorbent, which is at least partially returned to the absorption zone.
• Any dilute hydrochloric acid which is not saturated with hydrogen chloride is suitable as an absorbent.
• Their concentration c3 will usually be up to 25% by weight of hydrogen chloride, for example approximately 15% by weight.
• the absorption temperature is usually from 0 to 150 ° C., preferably from 30 to 100 ° C.
• the absorption pressure is usually from 0.5 to 20 bar, preferably from 1 to 10 bar.
• the desorption is preferably carried out in a desorption column with 3 to 10 theoretical floors.
• the uesorption pressure is usually from 0.3i ⁇ s 10 bar, preferably from 0.5 to 5 bar.
• a gas stream V is obtained which contains chlorine and oxygen or consists essentially of these gases. This usually contains traces of moisture.
• a drying step e) is therefore usually carried out, in which the gas stream V is freed from traces of moisture by contacting it with suitable drying agents.
• suitable drying agents are, for example, concentrated sulfuric acid, molecular sieves or hygroscopic adsorbents.
• an oxygen-containing stream is separated from the gas stream V, which stream can at least partially be returned to the oxidation zone as an oxygen-containing backflow Ila.
• the oxygen is preferably removed by distillation, customarily at a temperature in the range from -20 to +50 ° C. and a pressure in the range from 1 to 20 bar in a distillation column with 10 to 100 theoretical plates.
• the oxygen-containing backflow Ila is often under high pressure.
• FIG. 1 shows the process flow diagram of the process according to the invention in one embodiment.
• An oxygen-containing feed gas stream 1, a hydrogen chloride-containing feed stream 2, an oxygen-containing backflow 17 and a backflow 6a, which contains products of the hydrogen chloride oxidation, are fed into the hydrogen chloride oxidation reactor 3, in which hydrogen chloride is catalytically oxidized to chlorine.
• the propulsion jet nozzle 4 By means of the propulsion jet nozzle 4, the backflow 6a is sucked in by the oxygen-containing stream 1 and these are fed together into the reactor 3 as a gas stream 5.
• 94 vol.% Oxygen from pressure swing absorption (technically pure oxygen) or oxygen obtained by air liquefaction is used as the feed gas stream 1. This is under a high pressure, for example of 30 bar.
• a product gas stream 6 is obtained which contains chlorine, unreacted oxygen, unreacted hydrogen chloride and water vapor.
• the product gas stream 6 is separated into the recycle stream 6a and the product gas stream 6b for further processing.
• the product gas stream 6b is introduced into a quench cooler 7 in order to condense out hydrochloric acid 9.
• Water 8 can optionally be fed into the quench cooler as a quenching agent and a partial stream 9a of the dilute hydrochloric acid can be returned to the quench cooler as a quenching agent.
• Quench cooler 7 leaves a stream 10 of chlorine, oxygen and water vapor which is essentially freed from hydrogen chloride and which is fed to a drying stage 11.
• the gas stream 10 is brought into contact with a suitable absorbent such as sulfuric acid, molecular sieves or other hygroscopic adsorbents and thus freed from traces of water.
• a suitable absorbent such as sulfuric acid, molecular sieves or other hygroscopic adsorbents and thus freed from traces of water.
• the drying stage 11 is followed by a DeMister 13, in which the dried gas stream 12 is freed of entrained liquid particles.
• a de-mister is preferably provided if the drying stage 11 contains an absorption of sulfuric acid.
• the dried gas stream 14, which is optionally freed of liquid particles and consists of chlorine and oxygen, is fed to the distillation stage 15, in which oxygen is separated off and returned to the hydrogen chloride oxidation reactor as the backflow 17. It becomes a product stream 16 obtained from chlorine.
• a purge stream 17a is provided in order to avoid the build-up of inert gas components such as stic argon (possibly from
• FIG. 2 shows a variant of the method according to FIG. 1, in which the backflow 17 containing oxygen is used to draw in a further backflow 6c by means of a second propulsion jet nozzle 4b.
• FIG. 3 shows a further variant of the method according to FIG. 1.
• the product gas stream 6b is introduced into a phase contact apparatus 7 and brought into contact with dilute hydrochloric acid 20a and optionally water there.
• the stream 9 of highly concentrated hydrochloric acid loaded with the separated hydrogen chloride is fed to the desorption column 18, in which the absorbed hydrogen chloride is released again and is fed to the hydrogen chloride oxidation reactor 5 as a backflow 19.
• the dilute hydrochloric acid 20 obtained in the desorption is partly returned to the phase contact apparatus 7 and partly fed to a distillation column 21. There is distilled under reduced pressure to break the azeotrope. Water 22 and concentrated hydrochloric acid 23 are obtained, which is returned to the desorption column 18 in order to release further hydrogen chloride.

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• 2002
  • 2002-09-12 DE DE10242400A patent/DE10242400A1/de not_active Withdrawn
  • 2002-11-20 US US10/299,725 patent/US6962682B2/en not_active Expired - Fee Related
• 2003
  • 2003-09-12 JP JP2004537074A patent/JP4372008B2/ja not_active Expired - Fee Related
  • 2003-09-12 MX MXPA05002149A patent/MXPA05002149A/es active IP Right Grant
  • 2003-09-12 AU AU2003277856A patent/AU2003277856A1/en not_active Abandoned
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  • 2003-09-12 KR KR1020057004290A patent/KR100985127B1/ko not_active IP Right Cessation
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  • 2003-09-12 ES ES03769275T patent/ES2254975T3/es not_active Expired - Lifetime
  • 2003-09-12 EP EP03769275A patent/EP1542923B1/de not_active Expired - Lifetime
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